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Antimelanoma and Antityrosinase from Alpinia galangal Constituents

Two compounds, 1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one (BHPHTO) and bisdemethoxycurcumin (BDMC) they have been isolated from the rhizomes of Alpinia galangal, and the structures of both pure constituents were determined using spectroscopic analyses. The study examined the bioeffectivenesses...

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Autores principales: Lo, Chih-Yu, Liu, Po-Len, Lin, Li-Ching, Chen, Yen-Ting, Hseu, You-Cheng, Wen, Zhi-Hong, Wang, Hui-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763262/
https://www.ncbi.nlm.nih.gov/pubmed/24027439
http://dx.doi.org/10.1155/2013/186505
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author Lo, Chih-Yu
Liu, Po-Len
Lin, Li-Ching
Chen, Yen-Ting
Hseu, You-Cheng
Wen, Zhi-Hong
Wang, Hui-Min
author_facet Lo, Chih-Yu
Liu, Po-Len
Lin, Li-Ching
Chen, Yen-Ting
Hseu, You-Cheng
Wen, Zhi-Hong
Wang, Hui-Min
author_sort Lo, Chih-Yu
collection PubMed
description Two compounds, 1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one (BHPHTO) and bisdemethoxycurcumin (BDMC) they have been isolated from the rhizomes of Alpinia galangal, and the structures of both pure constituents were determined using spectroscopic analyses. The study examined the bioeffectivenesses of the two compounds on the human melanoma A2058 and showed that significantly inhibited the proliferation of melanoma cells in the cell viability assay. This research was also taken on the tests to B16-F10 cell line and showed minor inhibitory consequences of cellular tyrosinase activities and melanin contents. Our results revealed the anticancer effects of A. galangal compounds, and therefore, the target compounds could be potentially applied in the therapeutic application and the food industry.
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spelling pubmed-37632622013-09-11 Antimelanoma and Antityrosinase from Alpinia galangal Constituents Lo, Chih-Yu Liu, Po-Len Lin, Li-Ching Chen, Yen-Ting Hseu, You-Cheng Wen, Zhi-Hong Wang, Hui-Min ScientificWorldJournal Research Article Two compounds, 1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one (BHPHTO) and bisdemethoxycurcumin (BDMC) they have been isolated from the rhizomes of Alpinia galangal, and the structures of both pure constituents were determined using spectroscopic analyses. The study examined the bioeffectivenesses of the two compounds on the human melanoma A2058 and showed that significantly inhibited the proliferation of melanoma cells in the cell viability assay. This research was also taken on the tests to B16-F10 cell line and showed minor inhibitory consequences of cellular tyrosinase activities and melanin contents. Our results revealed the anticancer effects of A. galangal compounds, and therefore, the target compounds could be potentially applied in the therapeutic application and the food industry. Hindawi Publishing Corporation 2013-08-21 /pmc/articles/PMC3763262/ /pubmed/24027439 http://dx.doi.org/10.1155/2013/186505 Text en Copyright © 2013 Chih-Yu Lo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lo, Chih-Yu
Liu, Po-Len
Lin, Li-Ching
Chen, Yen-Ting
Hseu, You-Cheng
Wen, Zhi-Hong
Wang, Hui-Min
Antimelanoma and Antityrosinase from Alpinia galangal Constituents
title Antimelanoma and Antityrosinase from Alpinia galangal Constituents
title_full Antimelanoma and Antityrosinase from Alpinia galangal Constituents
title_fullStr Antimelanoma and Antityrosinase from Alpinia galangal Constituents
title_full_unstemmed Antimelanoma and Antityrosinase from Alpinia galangal Constituents
title_short Antimelanoma and Antityrosinase from Alpinia galangal Constituents
title_sort antimelanoma and antityrosinase from alpinia galangal constituents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763262/
https://www.ncbi.nlm.nih.gov/pubmed/24027439
http://dx.doi.org/10.1155/2013/186505
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